Canonical Allele Identifier: CA983862640
Gene: RPL27 HGNC NCBI

Linked Data

dbSNP Id: rs2050325385

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42998643_42998644del , CM000679.2:g.42998643_42998644del GRCh38
NC_000017.10:g.41150660_41150661del , CM000679.1:g.41150660_41150661del GRCh37
NC_000017.9:g.38404186_38404187del NCBI36
NG_053099.1:g.5371_5372del

Transcript Alleles

HGVS Amino-acid Change
ENST00000253788.12:c.-2-106_-2-105del MANE Select ENSP00000253788.5:n.-2-106_-2-105del
ENST00000589913.6:c.-108_-107del ENSP00000464813.1:n.-108_-107del
ENST00000253788.9:c.-2-106_-2-105del ENSP00000253788.4:n.-2-106_-2-105del
ENST00000587478.1:n.54-106_54-105del
ENST00000588830.1:c.-2-106_-2-105del ENSP00000468468.1:n.-2-106_-2-105del
ENST00000589037.5:c.-2-106_-2-105del ENSP00000467587.1:n.-2-106_-2-105del
ENST00000589913.5:c.-108_-107del ENSP00000464813.1:n.-108_-107del
ENST00000593262.1:n.225_226del
NM_000988.3:c.-2-106_-2-105del NP_000979.1:n.-2-106_-2-105del
NM_000988.5:c.-2-106_-2-105del MANE Select NP_000979.1:n.-2-106_-2-105del
NM_001349921.1:c.-2-106_-2-105del NP_001336850.1:n.-2-106_-2-105del
NM_001349922.1:c.-108_-107del NP_001336851.1:n.-108_-107del
NR_146327.1:n.82-106_82-105del
NM_001349921.2:c.-2-106_-2-105del NP_001336850.1:n.-2-106_-2-105del
NM_001349922.2:c.-108_-107del NP_001336851.1:n.-108_-107del
NR_146327.2:n.54-106_54-105del